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HRID 2424959作成日:2026年10月27日

Water → 7-Propyl-3-(trifluoromethyl)benzo[d]isoxazol-6-ol

https://huagongshe.com/reaction/2424959

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物TriphenylphosphineHCID 11776—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物1-(2,4-Dihydroxy-3-propylphenyl)-2,2,2-trifluoroethanone oximeHCID 136340076—
溶媒TetrahydrofuranHCID 8028—
生成物7-Propyl-3-(trifluoromethyl)benzo[d]isoxazol-6-olHCID 135800812—

反応条件

温度0 °C

反応手順

1-(2,4-Dihydroxy-3-propylphenyl)-2,2,2-trifluoroethanone oxime (prepared by the method described in WO 97/28137, 4.2 g, 15.96 mmol) and triphenylphosphine (8.82 g, 33.6 mmol) were dissolved in THF (250 mL) and the mixture was cooled to 0° C. A solution of diethyl azodicarboxylate (5.02 mL, 32.0 mmol) in THF (150 mL) was then slowly added over a period of 30 minutes. The reaction mixture was stirred for 1 h at 0° C. After addition of water (500 mL), the aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with brine and dried over sodium sulfate. The solvent was removed in vacuo and the product purified via silica gel flash chromatography (ethyl acetate/hexane (v/v)=1:6). The product was obtained as a white-yellow powder in a yield of 1.96 g (8.0 mmol, 50%). 1H NMR (300 MHz, CDCl3) δ 1.00 (t, 3H), 1.73 (m, 2H), 2.88 (t, 2H), 5.34 (s, 1H), 6.93 (d, 1H), 7.48 (d, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07964622B2
出典データセットuspto-grants-2011_06
ORD IDord-e154249f3a26420eb9731b55f02b8e65
出典メモuspto-grants-2011_06